63 research outputs found

    Probing polydopamine adhesion to protein and polymer films: microscopic and spectroscopic evaluation

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    Polydopamine has been found to be a biocompatible polymer capable of supporting cell growth and attachment, and to have antibacterial and antifouling properties. Together with its ease of manufacture and application, it ought to make an ideal biomaterial and function well as a coating for implants. In this paper, atomic force microscopy was used to measure the adhesive forces between polymer-, protein- or polydopamine-coated surfaces and a silicon nitride or polydopamine-functionalised probes. Surfaces were further characterised by contact angle goniometry, and solutions by circular dichroism. Polydopamine was further characterised with infrared spectroscopy and Raman spectroscopy. It was found that polydopamine functionalisation of the atomic force microscope probe significantly reduced adhesion to all tested surfaces. For example, adhesion to mica fell from 0.27 ± 0.7 nN nm-1 to 0.05 ± 0.01 nN nm-1. The results suggest that polydopamine coatings are suitable to be used for a variety of biomedical applications

    Abstracts from the Food Allergy and Anaphylaxis Meeting 2016

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    Unravelling electrochemical lignin depolymerization

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    Lignin valorisation via electrochemical depolymerization is a promising approach for commercial application due to its moderate reaction conditions. However, there is no available kinetics model for this reaction. Conventional reaction kinetics equations are inadequate when used for lignin degradation because of the limited kinetics information with respect the reaction mechanism. We suggest to use population balance equations to predict the evolution of molecular weight distribution of lignin with time. Solving the low molecular weight (MW) population balance equations is carried out discretely whereas a continuous solution was implemented for the high MW. Additionally, the model accounts for a recombination reaction for the depolymerized species. The model is capable of predicting the molecular weight distribution of lignin as a function of electrochemical processing time. New experimental results are used to extract kinetics constants for different kraft lignin samples
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